RIDDLE syndrome
human disease
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RIDDLE syndrome
Summary
RIDDLE syndrome is a developmental defect during embryogenesis[1]. It draws 100 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).[2]
Key Facts
- RIDDLE syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- RIDDLE syndrome's instance of is recorded as rare disease[4].
- RIDDLE syndrome's instance of is recorded as class of disease[5].
- RIDDLE syndrome is a type of autosomal recessive disease[6].
- RIDDLE syndrome is a type of autosomal recessive cerebellar ataxia[7].
- RIDDLE syndrome is a type of autosomal recessive cerebellar ataxia due to a DNA repair defect[8].
- RIDDLE syndrome is a type of DNA repair defect other than combined T-cell and B-cell immunodeficiencies[9].
- RIDDLE syndrome is a type of syndrome[10].
- RIDDLE syndrome's genetic association is recorded as RNF168[11].
- RIDDLE syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0090113[12].
- RIDDLE syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0090113[13].
- RIDDLE syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
Why It Matters
RIDDLE syndrome draws 100 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #135 of 308).[2] It is known by 6 alternative names across languages and contexts.[15]